A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5620760



Internal ID21569065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:67861810..67861810hg38UCSC Ensembl
chr1:68327493..68327493hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38346
hg19346
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17066062
SamplesHG03125
Known GenesGNG12-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5620760
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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